Pregnancy rates and outcomes in women with cystic fibrosis in the UK: comparisons with the general population before and after the introduction of disease‐modifying treatment, 2003... von Esan, OB, Schlüter, DK, Phillips, R, Cosgriff, R, Paranjothy, S, Williams, D, Norman, R, Carr, SB, Duckers, J, Taylor‐Robinson, D

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409 Improving data completion by moving to a new registry platform von Jeffery, A, Rajabzadeh-Heshejin, V, Cosgriff, R

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Identifying children with Cystic Fibrosis in population-scale routinely collected data in Wales: A Retrospective Review von Griffiths, R, Schlüter, D K, Akbari, A, Cosgriff, R, Tucker, D, Taylor-Robinson, D

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Fair selection of participants in clinical trials: The challenge to push the envelope further von Davies, J.C, Scott, S, Dobra, R, Brendell, R, Brownlee, K, Carr, S.B, Cosgriff, R, Simmonds, N.J, Jahan, R, Jones, A, Matthews, J, Brown, S, Galono, K, Miles, K, Pao, C, Shafi, N, Watson, D, Orchard, C, Davies, G, Pike, K, Shah, S, Bossley, C.J, Fong, T, Macedo, P, Ruiz, G, Waller, M, Baker, L

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Clinical characteristics of SARS-CoV-2 infection in children with cystic fibrosis: An international observational study von Bain, Robert, Cosgriff, Rebecca, Zampoli, Marco, Elbert, Alexander, Burgel, Pierre-Régis, Carr, Siobhán B, Castaños, Claudio, Colombo, Carla, Corvol, Harriet, Faro, Albert, Goss, Christopher H, Gutierrez, Hector, Jung, Andreas, Kashirskaya, Nataliya, Marshall, Bruce C, Melo, Joel, Mondejar-Lopez, Pedro, de Monestrol, Isabelle, Naehrlich, Lutz, Padoan, Rita, Pastor-Vivero, Maria Dolores, Rizvi, Samar, Salvatore, Marco, Filho, Luiz Vicente Ribeiro Ferreira da Silva, Brownlee, Keith G, Haq, Iram J, Brodlie, Malcolm

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P067 Using a national cystic fibrosis Registry to explore longitudinal outcome measures at an adult cystic fibrosis centre in comparison with other centres von Barry, P., Lee, A., Charman, S., Cosgriff, R., Jones, A.

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P072 Using Registry data to investigate differences in casemix and health indicators at an adult centre versus national peers von Jones, A., Cosgriff, R., Lee, A., Charman, S., Barry, P.

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Survival estimates in European cystic fibrosis patients and the impact of socioeconomic factors: a retrospective registry cohort study von McKone, Edward F., Ariti, Cono, Jackson, Abaigeal, Zolin, Anna, Carr, Siobhan B., Orenti, Annalisa, van Rens, Jacqui G., Lemonnier, Lydie, Macek, Milan, Keogh, Ruth H., Naehrlich, Lutz

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Clinical registries: governance, management, analysis and applications von Hickey, Graeme L, Grant, Stuart W, Cosgriff, Rebecca, Dimarakis, Ioannis, Pagano, Domenico, Kappetein, Arie P, Bridgewater, Ben

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P082 UK Cystic Fibrosis Registry data validation programme von Gunn, E., Caine, N., Cosgriff, R., Charman, S.C., Carr, S.B.

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Effects of acute hormone therapy on recurrent ischemia in postmenopausal women with unstable angina von Schulman, Steven P, Thiemann, David R, Ouyang, Pamela, Chandra, Nisha C, Schulman, Douglas S, Reis, Steven E, Terrin, Michael, Forman, Sandra, Piva de Albuquerque, Cicero, Bahr, Raymond D, Townsend, Susan N, Cosgriff, Rosalie, Gerstenblith, Gary

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P066 Development of an online tool to provide accessible and personalised information on life expectancy in cystic fibrosis von Tanner, K., Malik, F., Smith, T., Cosgriff, R., Medhurst, N., Keogh, R.

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P065 Perspectives on personalised life expectancy information and how it should be presented: a qualitative study von Malik, F., Tanner, K., Smith, T., Cosgriff, R., Medhurst, N., Keogh, R.

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WS23.4 Investigating associations between air pollution and the severity of cystic fibrosis in Great Britain von Khan, M. Saleem, Simmonds, N.J., Toledano, M.B., Cosgriff, R., Piel, F.B.

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P408 Patient preferences regarding lung transplant referral von Medhurst, N., Cosgriff, R., Dunk, R., Evans, A., Francis, C., Madge, S., Schlüter, D., Keogh, R.

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P071 Linkage of the UK cystic fibrosis Registry with electronic health records in Wales: a new resource for research von Griffiths, R., Schlüter, D.K., Akbari, A., Cosgriff, R., Tucker, D.F., Taylor-Robinson, D.

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WS10-2 Investigating differences in outcomes in people with cystic fibrosis with a nonsense mutation, compared to the total cystic fibrosis patient population and patients homozygo... von Carr, S., Carroll, O., Cunningham, S., Simmonds, N., Cosgriff, R., Newsome, S., Keogh, R.

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P085 Investigating time between annual review encounters in the UK Cystic Fibrosis Registry von McClenaghan, E., Cosgriff, R., Yip, M., Charman, S.C., Lee, A., Gunn, E., Earlam, K.

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WS10-6 The UK cystic fibrosis transplant pathway: from evaluation to post-transplant survival using Registry data von Keogh, R.H., Schluter, D.K., Carr, S., Charman, S.C., Cosgriff, R., Medhurst, N., Simmonds, N.J.

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WS08.1 Pregnancy and perinatal outcomes in women with cystic fibrosis in the UK: a population-based study using UK Registry data, 2003–2017 von Esan, O.B., Schlüter, D.K., Phillips, R., Cosgriff, R., Paranjothy, S., Williams, D., Norman, R., Carr, S.B., Duckers, J., Taylor-Robinson, D.

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